{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-08-13",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "41953",
      "product_res_number": "Z-0124-06",
      "event_date_initiated": "2005-08-31",
      "event_date_posted": "2005-11-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-05-09",
      "res_event_number": "33490",
      "product_code": "DTA",
      "k_numbers": [
        "K050884"
      ],
      "product_description": "Model 6149 Pacing Vector Selector Cable Switch for use with Pacing System Analyzers * Rx only * Contents Are Not Sterile * Manufactured by Remington Medical Incorporated, 6830 Meadowridge Court, Alpharetta, GA 30005, (770) 888-8520 or (800) 999-0057 * Distributed By: Guidant Corporation, 4100 Hamine Avenue North, St. Paul, MN 55112-5798 USA.",
      "code_info": "Lot number: 051781, 051782, 051783, 051788, 0517939.",
      "firm_fei_number": "1000132370",
      "recalling_firm": "Remington Medical Inc.",
      "address_1": "6830 Meadowridge Ct",
      "city": "Alpharetta",
      "state": "GA",
      "postal_code": "30005-2202",
      "additional_info_contact": "Maria Granito\n770-989-0057",
      "reason_for_recall": "The vector selector has an electrical design flaw which prevents RV pacing.",
      "root_cause_description": "Other",
      "action": "Guidant Corporation notified Remington Medical of the problem. Remington had instructed Guidant to retrieve the product from their sales force by 09/07/2005 and return to Remington by 09/09/2005.",
      "product_quantity": "600 units",
      "distribution_pattern": "MN",
      "openfda": {
        "k_number": [
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          "K050884",
          "K791380",
          "K073230",
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        "device_name": "Tester, Pacemaker Electrode Function",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.3720",
        "device_class": "2"
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}